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Freelance Medical Device Technical Writer Jobs (NOW HIRING)

Orion Group

$33 - $38/hr

Senior Technical Writer - Quality Documentation & Change Control Location: 100% Onsite- Branchburg ... Pharmaceutical / Medical Device / Biotechnology Contract through the end of 2026 with potential ...

The Contingent Plan

Technical Writer II

San Diego, CA · On-site

Pharmaceutical and/or medical device experience preferred. * Understanding of cGMP, ISO13485, and regulatory requirements * Three years of experience working as a technical writer. * Project ...

Adecco

Technical Writer

Carlsbad, CA · On-site

$33/hr

Technical Writer - Manufacturing Sciences Location: Carlsbad, CA Pay Rate: $33.00 per hour Position ... Experience working in a pharmaceutical, biotechnology, medical device, or other regulated ...

Abbott Laboratories

Technical Writer

Des Plaines, IL · On-site

$61 - $123/hr

... medical device product lines. * Communicate with other writers, engineers, scientists, product managers, etc., to develop and understand technical content. * Assists in document format and layout.

MiniMed

Technical Writer

Los Angeles, CA · On-site

$64K - $110K/yr

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Develop of a working understanding of medical device products * Work with required subject matter ...

MiniMed

Technical Writer

Minneapolis, MN · On-site

$64K - $110K/yr

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Develop of a working understanding of medical device products * Work with required subject matter ...

Abbott

Technical Writer

Des Plaines, IL · On-site

$61K - $122K/yr

... medical device product lines. * Communicate with other writers, engineers, scientists, product managers, etc., to develop and understand technical content. * Assists in document format and layout.

Collabera

Technical writer

Eagan, MN · On-site

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... We are looking for a freelance/contractor Technical Writer to produce high-quality documentation.

Automated Systems, Inc.

GMP Technical Writer

Madison, WI · On-site

$69 - $96/hr

Requirements RequiredQualifications & Experience * 4+ years of GMP technical writing experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.

MiniMed

Technical Writer

Atlanta, GA · On-site

$64K - $110K/yr

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Develop of a working understanding of medical device products * Work with required subject matter ...

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Freelance Medical Device Technical Writer information

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How much do freelance medical device technical writer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for freelance medical device technical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.
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Freelance Medical Device Technical Writer jobs near you
Infographic showing various Freelance Medical Device Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Technical Writer

Stark Pharma Solutions Inc

Swiftwater, PA • On-site

Contractor

Re-posted 26 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Technical Writer

Location: Swiftwater, PA

Duration: 6-Month Contract

Industry: Pharmaceutical / Biotech Manufacturing

Position Overview

We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical and quality-related content into user-friendly training materials and documentation. This role will work closely with cross-functional teams to create compliant documentation, training content, and process materials within a GMP-regulated environment.

The ideal candidate will have experience in technical writing, quality systems documentation, and digital system deployments within pharmaceutical, biotechnology, laboratory, or manufacturing environments.

Key Responsibilities

  • Develop, revise, and maintain technical documentation, training materials, and process-related content.
  • Convert technical and operational information into engaging training presentations, user guides, and instructional materials.
  • Review, edit, and update quality documents including:
  • Standard Operating Procedures (SOPs)
  • Work Instructions
  • Guidelines
  • Validation Master Plans
  • Quality System Documentation
  • Ensure all documentation complies with GMP, regulatory, and internal quality requirements.
  • Collaborate with Quality, IT, Laboratory, and Operations teams to gather information and create accurate documentation.
  • Support digital transformation initiatives by developing training materials for new system implementations.
  • Assist with document control activities and quality documentation updates.
  • Create visual content, process flows, diagrams, and presentations using PowerPoint and Visio.
  • Participate in training development and delivery activities as needed.

Required Qualifications

  • Bachelor's degree required; advanced degrees (Master's or PhD) are welcome.
  • Minimum 2+ years of experience in Technical Writing, Documentation Management, or a related role.
  • Experience working within GMP-regulated pharmaceutical, biotech, laboratory, or life sciences environments.

Hands-on experience with quality systems and applications such as:

  • Veeva
  • LIMS
  • LabWare (preferred)

Proficiency with:

  • Microsoft Word
  • Excel
  • PowerPoint
  • Visio
  • Outlook
  • Strong technical writing, editing, and document management skills.
  • Excellent verbal and written communication abilities.
  • Strong interpersonal skills with the ability to work effectively in cross-functional teams.